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Updated: Jan 24, 2026

Development of a Hepatitis B Virus Reporter System to Monitor the Early Stages of the Replication Cycle
Published on: February 1, 2017
Long-Term Follow-up and Quantitative Hepatitis B Surface Antigen Monitoring in North American Chronic HBV Carriers
Conar R O'Neil1, Stephen E Congly2, M Sarah Rose3
1Division of Infectious Disease, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, Alberta, Canada; Department of Internal Medicine, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
Insights
Quantitative hepatitis B surface antigen (qHBsAg) levels correlate with chronic hepatitis B (CHB) phases. In patients on long-term nucleoside analogue (NA) therapy, qHBsAg levels stabilize, with some achieving low levels potentially allowing treatment discontinuation.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Quantitative hepatitis B surface antigen (qHBsAg) is a potential biomarker for chronic hepatitis B (CHB) management.
- Understanding qHBsAg dynamics across disease phases and treatment is crucial for optimizing patient care.
Purpose of the Study:
- To evaluate qHBsAg levels in relation to CHB disease phases in untreated patients.
- To assess qHBsAg level changes over time in patients receiving nucleoside analogue (NA) therapy.
Main Methods:
- Retrospective cohort study of 545 CHB carriers.
- Analysis of qHBsAg levels stratified by CHB disease phase (immune tolerant, immune clearance, inactive, HBeAg-negative).
- Longitudinal qHBsAg assessment in patients treated with entecavir, tenofovir, or lamivudine.
Main Results:
- Significant differences in median qHBsAg levels were observed across untreated CHB phases (p < 0.001).
- In the NA-treated cohort, qHBsAg levels remained stable over time.
- Sustained low qHBsAg (< 2 log10 IU/mL) was observed in 19% of patients on long-term NA therapy.
Conclusions:
- qHBsAg levels are associated with CHB disease phase and treatment status.
- Stable qHBsAg titers in long-term NA-treated patients suggest a potential marker for treatment discontinuation assessment.
- A subset of treated patients with low qHBsAg may be candidates for stopping NA therapy without increased risk of hepatitis flares.
Introduction:
Quantitative hepatitis B surface antigen (qHBsAg) combined with HBV DNA may be useful for predicting chronic hepatitis B (CHB) activity and nucleoside analogue (NA) response.
Material And Methods:
In this retrospective cohort study we evaluated qHBsAg levels according to CHB disease phase and among patients on treatment. Random effect logistic regression analysis was used to analyze qHBsAg change with time in the NA-treated cohort.
Results:
545 CHB carriers [56% M, median age 48 y (IQR 38-59), 73% Asian] had qHBsAg testing. In the untreated group (44%), 8% were classified as immune tolerant, 10% immune clearance, 40% inactive, and 43% had HBeAg- CHB and the median HBsAg levels were 4.6 (IQR 3.4-4.9), 4.0 (IQR 3.4-4.5), 2.9 (IQR 1.4-3.8), and 3.2 log IU/mL (IQR 2.6-4.0), respectively; p < 0.001. In the NA-treated group (28% entecavir, 68% tenofovir, 4% lamivudine), no significant change in qHBsAg levels occured with time. However, 19% of patients on long-term NA had sustained qHBsAg < 2 log10 IU/mL.
Conclusion:
qHBsAg titers were associated with CHB phase and remained stable in those on long-term NA. A significant number of treated patients had low-level qHBsAg, of which some may be eligible for treatment discontinuation without risk of flare.
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